Cargando…
Synthesis of a new fluorophore: wavelength-tunable bisbenzo[f]isoindolylidenes
The creation of new functional molecules is a central task in chemical synthesis. Herein, we report the synthesis of a new type of fluorophore, bisbenzo[f]isoindolylidenes, from easily accessible dipropargyl benzenesulfonamides. Wavelength-tunable fluorophores emitting strong fluorescence of green t...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10664550/ https://www.ncbi.nlm.nih.gov/pubmed/38023512 http://dx.doi.org/10.1039/d3sc04445a |
_version_ | 1785138642154422272 |
---|---|
author | Ye, Changqing Huang, Rui Chiou, Mong-Feng Wang, Bo Li, Daliang Bao, Hongli |
author_facet | Ye, Changqing Huang, Rui Chiou, Mong-Feng Wang, Bo Li, Daliang Bao, Hongli |
author_sort | Ye, Changqing |
collection | PubMed |
description | The creation of new functional molecules is a central task in chemical synthesis. Herein, we report the synthesis of a new type of fluorophore, bisbenzo[f]isoindolylidenes, from easily accessible dipropargyl benzenesulfonamides. Wavelength-tunable fluorophores emitting strong fluorescence of green to red light were obtained in this reaction. Late-stage modifications and incorporation of bioactive molecules into these fluorophores give rise to potential applications in biological studies. Detailed computational and experimental studies were conducted to elucidate the mechanism, and suggest a reaction sequence involving Garratt–Braverman type cyclization, isomerization, fragmentation, dimerization and oxidation. |
format | Online Article Text |
id | pubmed-10664550 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-106645502023-11-02 Synthesis of a new fluorophore: wavelength-tunable bisbenzo[f]isoindolylidenes Ye, Changqing Huang, Rui Chiou, Mong-Feng Wang, Bo Li, Daliang Bao, Hongli Chem Sci Chemistry The creation of new functional molecules is a central task in chemical synthesis. Herein, we report the synthesis of a new type of fluorophore, bisbenzo[f]isoindolylidenes, from easily accessible dipropargyl benzenesulfonamides. Wavelength-tunable fluorophores emitting strong fluorescence of green to red light were obtained in this reaction. Late-stage modifications and incorporation of bioactive molecules into these fluorophores give rise to potential applications in biological studies. Detailed computational and experimental studies were conducted to elucidate the mechanism, and suggest a reaction sequence involving Garratt–Braverman type cyclization, isomerization, fragmentation, dimerization and oxidation. The Royal Society of Chemistry 2023-11-02 /pmc/articles/PMC10664550/ /pubmed/38023512 http://dx.doi.org/10.1039/d3sc04445a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Ye, Changqing Huang, Rui Chiou, Mong-Feng Wang, Bo Li, Daliang Bao, Hongli Synthesis of a new fluorophore: wavelength-tunable bisbenzo[f]isoindolylidenes |
title | Synthesis of a new fluorophore: wavelength-tunable bisbenzo[f]isoindolylidenes |
title_full | Synthesis of a new fluorophore: wavelength-tunable bisbenzo[f]isoindolylidenes |
title_fullStr | Synthesis of a new fluorophore: wavelength-tunable bisbenzo[f]isoindolylidenes |
title_full_unstemmed | Synthesis of a new fluorophore: wavelength-tunable bisbenzo[f]isoindolylidenes |
title_short | Synthesis of a new fluorophore: wavelength-tunable bisbenzo[f]isoindolylidenes |
title_sort | synthesis of a new fluorophore: wavelength-tunable bisbenzo[f]isoindolylidenes |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10664550/ https://www.ncbi.nlm.nih.gov/pubmed/38023512 http://dx.doi.org/10.1039/d3sc04445a |
work_keys_str_mv | AT yechangqing synthesisofanewfluorophorewavelengthtunablebisbenzofisoindolylidenes AT huangrui synthesisofanewfluorophorewavelengthtunablebisbenzofisoindolylidenes AT chioumongfeng synthesisofanewfluorophorewavelengthtunablebisbenzofisoindolylidenes AT wangbo synthesisofanewfluorophorewavelengthtunablebisbenzofisoindolylidenes AT lidaliang synthesisofanewfluorophorewavelengthtunablebisbenzofisoindolylidenes AT baohongli synthesisofanewfluorophorewavelengthtunablebisbenzofisoindolylidenes |